Džidić-Krivić Amina, Fajkić Almir, Farhat Esma Karahmet, Lekić Lana, Ejubović Amira, Vukas Samra Kadić, Ejubović Malik, Lepara Orhan, Sher Emina Karahmet
Department of Neurology, Cantonal Hospital Zenica, 72000, Zenica, Bosnia and Herzegovina.
Faculty of Medicine, University of Zenica, 72000, Zenica, Bosnia and Herzegovina.
Mol Neurobiol. 2025 Apr 24. doi: 10.1007/s12035-025-04947-w.
The global rise in both metabolic syndrome (MetS) and neurodegenerative diseases (NDs), particularly dementia and Alzheimer's disease (AD) poses a growing health and socioeconomic burden. MetS affects approximately 25% of the global adult population and is associated with insulin resistance, hypertension, dyslipidemia, and obesity, factors increasingly linked to cognitive impairment and brain atrophy. This review explores the shared pathophysiological mechanisms between MetS and NDs, including neuroinflammation, oxidative stress, insulin resistance in the brain, blood-brain barrier (BBB) dysfunction, mitochondrial damage, gut microbiota dysbiosis, and alterations in the renin-angiotensin system. In terms of substance, MetS patients are four times more likely to develop dementia, with increased markers such as CRP and IL-6 present in the patient populations. The review suggests the role of astrocytic insulin signalling, adipokines, and toll-like receptors as key molecular links. Interventions such as caloric restriction, hydroxytyrosol (HT), and intranasal insulin have shown promising outcomes at preclinical and early clinical stages. Antidiabetic drugs like metformin, liraglutide, and GLP-1 receptor agonists have the potential to modulate neuroinflammation and improve cognition. Angiotensin receptor blockers like losartan and candesartan also exhibit neuroprotection via RAS pathway modulation. The review emphasizes the need for longitudinal studies and clinical trials to confirm these therapeutic agents and develop effective and cost-friendly interventions for the prevention and management of neurodegeneration in patients with metabolic syndrome.
代谢综合征(MetS)和神经退行性疾病(NDs),尤其是痴呆症和阿尔茨海默病(AD)在全球范围内的发病率不断上升,给健康和社会经济带来了日益沉重的负担。MetS影响着全球约25%的成年人口,与胰岛素抵抗、高血压、血脂异常和肥胖相关,这些因素越来越多地与认知障碍和脑萎缩联系在一起。本综述探讨了MetS和NDs之间共同的病理生理机制,包括神经炎症、氧化应激、脑内胰岛素抵抗、血脑屏障(BBB)功能障碍、线粒体损伤、肠道微生物群失调以及肾素-血管紧张素系统的改变。在实质内容方面,MetS患者患痴呆症的可能性是正常人的四倍,患者群体中存在如CRP和IL-6等升高的标志物。该综述表明星形胶质细胞胰岛素信号传导、脂肪因子和Toll样受体作为关键分子联系的作用。热量限制、羟基酪醇(HT)和鼻内胰岛素等干预措施在临床前和临床早期阶段已显示出有前景的结果。二甲双胍、利拉鲁肽和GLP-1受体激动剂等抗糖尿病药物有可能调节神经炎症并改善认知。氯沙坦和坎地沙坦等血管紧张素受体阻滞剂也通过调节RAS途径表现出神经保护作用。该综述强调需要进行纵向研究和临床试验,以确认这些治疗药物,并开发出有效且经济实惠的干预措施,用于预防和管理代谢综合征患者的神经退行性变。